EP2736716A1 - Planarer verbundwerkstoff mit kunststoffschichten von unterschiedlicher vicat-weichmachertemperatur - Google Patents

Planarer verbundwerkstoff mit kunststoffschichten von unterschiedlicher vicat-weichmachertemperatur

Info

Publication number
EP2736716A1
EP2736716A1 EP12740891.2A EP12740891A EP2736716A1 EP 2736716 A1 EP2736716 A1 EP 2736716A1 EP 12740891 A EP12740891 A EP 12740891A EP 2736716 A1 EP2736716 A1 EP 2736716A1
Authority
EP
European Patent Office
Prior art keywords
layer
thermoplastic
layers
sheetlike composite
ksw
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP12740891.2A
Other languages
English (en)
French (fr)
Other versions
EP2736716B1 (de
Inventor
Michael Wolters
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
SIG Combibloc Services AG
Original Assignee
SIG Technology AG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=46598450&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=EP2736716(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by SIG Technology AG filed Critical SIG Technology AG
Priority to PL12740891T priority Critical patent/PL2736716T3/pl
Publication of EP2736716A1 publication Critical patent/EP2736716A1/de
Application granted granted Critical
Publication of EP2736716B1 publication Critical patent/EP2736716B1/de
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B65CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65DCONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
    • B65D5/00Rigid or semi-rigid containers of polygonal cross-section, e.g. boxes, cartons or trays, formed by folding or erecting one or more blanks made of paper
    • B65D5/42Details of containers or of foldable or erectable container blanks
    • B65D5/56Linings or internal coatings, e.g. pre-formed trays provided with a blow- or thermoformed layer
    • B65D5/563Laminated linings; Coatings
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B31MAKING ARTICLES OF PAPER, CARDBOARD OR MATERIAL WORKED IN A MANNER ANALOGOUS TO PAPER; WORKING PAPER, CARDBOARD OR MATERIAL WORKED IN A MANNER ANALOGOUS TO PAPER
    • B31BMAKING CONTAINERS OF PAPER, CARDBOARD OR MATERIAL WORKED IN A MANNER ANALOGOUS TO PAPER
    • B31B50/00Making rigid or semi-rigid containers, e.g. boxes or cartons
    • B31B50/74Auxiliary operations
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B15/00Layered products comprising a layer of metal
    • B32B15/04Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • B32B15/08Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B15/00Layered products comprising a layer of metal
    • B32B15/20Layered products comprising a layer of metal comprising aluminium or copper
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • B32B27/06Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • B32B27/08Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • B32B27/06Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • B32B27/10Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of paper or cardboard
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • B32B27/30Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers
    • B32B27/308Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers comprising acrylic (co)polymers
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • B32B27/32Layered products comprising a layer of synthetic resin comprising polyolefins
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • B32B27/32Layered products comprising a layer of synthetic resin comprising polyolefins
    • B32B27/327Layered products comprising a layer of synthetic resin comprising polyolefins comprising polyolefins obtained by a metallocene or single-site catalyst
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • B32B27/34Layered products comprising a layer of synthetic resin comprising polyamides
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B3/00Layered products comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar form; Layered products having particular features of form
    • B32B3/26Layered products comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar form; Layered products having particular features of form characterised by a particular shape of the outline of the cross-section of a continuous layer; characterised by a layer with cavities or internal voids ; characterised by an apertured layer
    • B32B3/266Layered products comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar form; Layered products having particular features of form characterised by a particular shape of the outline of the cross-section of a continuous layer; characterised by a layer with cavities or internal voids ; characterised by an apertured layer characterised by an apertured layer, the apertures going through the whole thickness of the layer, e.g. expanded metal, perforated layer, slit layer regular cells B32B3/12
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B7/00Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
    • B32B7/02Physical, chemical or physicochemical properties
    • B32B7/027Thermal properties
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B7/00Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
    • B32B7/04Interconnection of layers
    • B32B7/12Interconnection of layers using interposed adhesives or interposed materials with bonding properties
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B65CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65BMACHINES, APPARATUS OR DEVICES FOR, OR METHODS OF, PACKAGING ARTICLES OR MATERIALS; UNPACKING
    • B65B5/00Packaging individual articles in containers or receptacles, e.g. bags, sacks, boxes, cartons, cans, jars
    • B65B5/02Machines characterised by incorporation of means for making the containers or receptacles
    • B65B5/024Machines characterised by incorporation of means for making the containers or receptacles for making containers from preformed blanks
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2250/00Layers arrangement
    • B32B2250/055 or more layers
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2270/00Resin or rubber layer containing a blend of at least two different polymers
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00Properties of the layers or laminate
    • B32B2307/50Properties of the layers or laminate having particular mechanical properties
    • B32B2307/514Oriented
    • B32B2307/516Oriented mono-axially
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00Properties of the layers or laminate
    • B32B2307/70Other properties
    • B32B2307/718Weight, e.g. weight per square meter
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00Properties of the layers or laminate
    • B32B2307/70Other properties
    • B32B2307/724Permeability to gases, adsorption
    • B32B2307/7242Non-permeable
    • B32B2307/7244Oxygen barrier
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00Properties of the layers or laminate
    • B32B2307/70Other properties
    • B32B2307/724Permeability to gases, adsorption
    • B32B2307/7242Non-permeable
    • B32B2307/7246Water vapor barrier
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00Properties of the layers or laminate
    • B32B2307/70Other properties
    • B32B2307/726Permeability to liquids, absorption
    • B32B2307/7265Non-permeable
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2439/00Containers; Receptacles
    • B32B2439/40Closed containers
    • B32B2439/62Boxes, cartons, cases
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2439/00Containers; Receptacles
    • B32B2439/70Food packaging
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B65CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65DCONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
    • B65D5/00Rigid or semi-rigid containers of polygonal cross-section, e.g. boxes, cartons or trays, formed by folding or erecting one or more blanks made of paper
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/24Structurally defined web or sheet [e.g., overall dimension, etc.]
    • Y10T428/24942Structurally defined web or sheet [e.g., overall dimension, etc.] including components having same physical characteristic in differing degree

Definitions

  • the present invention generally relates to a sheetlike composite comprising a layer configuration with at least the following layers:
  • thermoplastic KSu a first layer of thermoplastic KSu
  • thermoplastic KSw a second layer of thermoplastic KSw
  • the present invention furthermore relates to a process for the production of the sheetlike composite, a container which surrounds an interior and comprises at least one such sheetlike composite, and a process for the production of this container which comprises the steps of provision of the sheetlike composite of abovementioned layer configuration, folding, joining and optionally filling and closing of the container obtained in this way.
  • the problems which arise during closing of the containers already filled with a foodstuff are, inter alia, the following:
  • the containers of the abovementioned type are as a rule closed by softening, superficial melting or liquefying the layers of plastic of the container.
  • These layers of plastic often have tacky properties in the softened, molten or liquid state, so that the container adheres to the closing tool in this tacky region. In addition to damage and defective packs, this also leads to expensive, shorter maintenance intervals for the closing tool.
  • the abovementioned difficulties during closing could thus be avoided if the temperature at the closing point were to be kept lower.
  • the tackiness of a substance in general decreases with decreasing temperature, which would lead to less adhesion of the containers to the closing tool. Nevertheless, closure points produced in this manner are often less tight, which in turn can lead to a reduced shelf life and reduced quality of the foodstuffs contained in the container.
  • the object of present invention is to at least partly eliminate the disadvantages emerging from the prior art.
  • the object of providing a sheetlike composite which, during closing by a closing tool, adheres to the closing tool as little as possible, preferably not at all.
  • An object according to the invention is furthermore to provide a container from a composite, wherein the container can be produced by easy folding of the composite and at the same time should have a high tightness.
  • the container should therefore be particularly well-suited to long-term storage of sensitive foodstuffs.
  • a further object is to provide a sheetlike composite which, during closing by a closing tool, adheres to the closing tool as little as possible, preferably not at all, and at the same time furthermore should have a high tightness in the sense of impermeability to liquid, vapour and oxygen.
  • a further object is to provide a sheetlike composite which has a sealing window which is as large as possible.
  • a further object is to provide a sheetlike composite which is suitable in particular for the production of containers for transportation and storage of foodstuffs, animal feeds, drinks of low carbonic acid content and the like.
  • a contribution towards achieving at least one of the above objects is made by a sheetlike composite comprising a layer configuration with at least the following layers:
  • thermoplastic KSu a first layer of thermoplastic KSu
  • KSw thermoplastic KSw
  • the sheetlike composite has at least one further layer of thermoplastic KSv, which is preferably provided between layer ii. and layer iv.;.
  • the Vicat softening temperature of the layer of thermoplastic KSu and preferably also the Vicat softening temperature of the layer of thermoplastic KSv is in each case higher than the Vicat softening temperature of the layer of thermoplastic KSw.
  • joint used in this description includes the adhesion of two objects beyond van der Waals forces of attraction. These objects can either follow one another directly or be joined to one another via further objects.
  • the carrier layer can be joined directly and therefore immediately to the layer of thermoplastic KSu, or can also be joined indirectly via an adhesion promoter layer, a direct joining being preferred.
  • the wording "comprising a layer configuration with at least 5 layers” as used above means that at least the stated layers can be present in the sheetlike composite according to the invention in the sequence shown. This wording does not necessarily mean that these layers follow one another directly. Rather, this wording includes constellations in which one or more additional layers can moreover be present between two layers mentioned successively in the above sequence. In a preferred embodiment of the sheetlike composite according to the invention, this contains at least one further layer of thermoplastic KSa, which is preferably present between layer ii. and layer iv., particularly preferably between layer iii. and layer iv.
  • a further layer or several further layers may also additionally be provided over the complete or a part of the area on the side of the layer of thermoplastic KSu facing the environment.
  • a printed layer may also be applied on the side of the layer of thermoplastic KSu facing the environment.
  • possible further layers are also covering or protective layers.
  • the layer of thermoplastic KSu itself could also be a covering or protective layer for the printed layer.
  • the sheetlike composite comprises at least one first layer of thermoplastic KSu, wherein this preferably has a weight per unit area in a range of from 5 to 50 g/m 2 , particularly preferably in a range of from 8 to 40 g/m 2 and most preferably in a range of from 10 to 30 g/m 2 .
  • the layer of thermoplastic KSu comprises a thermoplastic polymer to the extent of at least 70 wt.%, preferably at least 80 wt.% and particularly preferably at least 95 wt.%, in each case based on the layer of thermoplastic KSu.
  • all known thermoplastics which seem suitable to the person skilled in the art can be used for the layer of thermoplastic KSv.
  • thermoplastics of the layer of thermoplastic KSu are, in particular, those which can be easily processed due to good extrusion properties.
  • polymers obtained by chain polymerization are suitable, in particular polyesters or polyolefins, cyclic olefin copolymers (COC), polycyclic olefin copolymers (POC), in particular polyethylene and polypropylene, being particularly preferred and polyethylene being very particularly preferred.
  • COC cyclic olefin copolymers
  • POC polycyclic olefin copolymers
  • polyethylene and polypropylene being particularly preferred
  • polyethylene being very particularly preferred.
  • Mixtures of at least two thermoplastics can also be employed for the layer of thermoplastic KSu.
  • the polyethylenes HDPE, MDPE, LDPE, LLDPE, VLDPE and PE and mixtures of at least two of these are preferred according to the present invention.
  • Suitable polyethylenes have a melt flow rate (MFR) in a range of from 1 to 25 g/10 min, preferably in a range of from 2 to 20 g/10 min and particularly preferably in a range of from 2.5 to l5 g/10 min, and a density in a range of from 0.890 g/cm 3 to 0.980 g/cm 3 , preferably in a range of from 0.895 g/cm 3 to 0.975 g/cm 3 , and further preferably in a range of from 0.900 g/cm 3 to 0.970 g/cm 3 .
  • MFR melt flow rate
  • the at least one thermoplastic polymer contained in the layer of thermoplastic KSu preferably all the polymers contained in the layer of thermoplastic KSu, preferably has a melting temperature in a range of from 80 to 155 °C, preferably in a range of from 90 to 145 °C and particularly preferably in a range of from 95 to 135 °C.
  • the thermoplastic polymer has a Vicat softening temperature of at least 90 °C, preferably at least 95 °C and particularly preferably at least 100 °C.
  • This thermoplastic polymer furthermore preferably has a melting point of at least 110 °C, preferably at least 1 15 °C and particularly preferably at least 120 °C.
  • This thermoplastic polymer moreover preferably has a density of at least 0.918 g/cm 3 , preferably at least 0.922 g/cm 3 , particularly preferably at least 0.925 g/cm 3 and moreover preferably at least 0.930 g/cm 3 .
  • the layer of thermoplastic KSu is present as a mixture of at least two thermoplastics.
  • the layer of plastic KSu it is furthermore preferable for the layer of plastic KSu to comprise at least 25 wt.%, particularly preferably at least 35 wt.% and most preferably at least 45 wt.%, in each case based on the layer of thermoplastic KSu, of a thermoplastic which has a Vicat softening temperature of at least 90 °C, preferably at least 95 °C and particularly preferably at least 100 °C.
  • This thermoplastic furthermore preferably has a melting point of at least 110 °C, preferably more than 1 15 °C and particularly preferably at least 120 °C.
  • This thermoplastic moreover preferably has a density of at least 0.918 g/cm 3 , preferably at least 0.922 g/cm , particularly preferably at least 0.925 g/cm and moreover preferably at least 0.930 g/cm 3 .
  • the layer of thermoplastic KSu prefferably has a Vicat softening temperature in a range of from 90 °C to 150 °C, preferably from 95 °C to 140 °C and particularly preferably from 100 °C to 135 °C.
  • any material which is suitable for this purpose to the person skilled in the art and which has an adequate strength and rigidity to give the container stability to the extent that in the filled state the container essentially retains its shape can be employed.
  • plant-based fibrous substances in particular pulps, preferably sized, bleached and/or non-bleached pulps are preferred, paper and cardboard being particularly preferred.
  • the weight per unit area of the carrier layer is preferably in a range of from 120 to 450 g/m 2 , particularly preferably in a range of from 130 to 400 g/m 2 and most preferably in a range of from 150 to 380 g/m .
  • a preferred cardboard preferably as a rule has a single- or multilayer configuration and can be coated on one or both sides with one or also more covering layers.
  • a preferred cardboard furthermore has a residual moisture content of less than 20 wt.%, preferably from 2 to 15 wt.% and particularly preferably from 4 to 10 wt.%.
  • a particularly preferred cardboard has a multilayer configuration.
  • the cardboard furthermore preferably has at least one, but particularly preferably at least two layers of a covering layer, which is known to the person skilled in the art as "coating", on the surface facing the environment.
  • liquid phases comprising inorganic solid particles, preferably solutions containing chalk, gypsum or clay, which are applied to the surface of the cardboard are usually called a "coating".
  • a preferred cardboard furthermore preferably has a Scott bond value in a range of from 100 to 350 J/m , preferably from 125 to 330 J/m and particularly preferably from 135 to 310 J/m . Due to the abovementioned ranges, it is possible to provide a composite from which a container of high tightness can be folded easily and in low tolerances.
  • the layer of thermoplastic KSv preferably lies between layer ii. and layer iv.
  • the layer of thermoplastic KSv lies between layer ii. and layer iii.
  • the layer of thermoplastic KSv preferably following layer ii. directly, and preferably being joined to layer iii. indirectly, for example via an adhesion promoter layer.
  • the layer of thermoplastic KSv lies between layer iii. and layer iv.
  • the layer of thermoplastic KSv is preferably joined directly to layer iv. and is preferably joined indirectly, for example via an adhesion promoter layer, to layer iii.
  • the layer of thermoplastic KSv preferably has a weight per unit area in a range of from 5 to
  • thermoplastic KSu particularly preferably in a range of from 8 to 30 g/m and moreover preferably in a range of from 10 to 25 g/m .
  • the plastics which have already been described above for the layer of thermoplastic KSu, in particular, can preferably be employed.
  • the layer of thermoplastic KSv has at least one thermoplastic polymer which has a Vicat softening temperature of at least 90 °C, preferably at least 95 °C and particularly preferably at least 100 °C.
  • This thermoplastic polymer furthermore preferably has a melting point of at least 1 10 °C, preferably at least 1 15 °C and particularly preferably at least 120 °C.
  • This thermoplastic polymer moreover preferably has a density of at least 0.918 g/cm 3 , preferably at least 0.922 g/cm 3 , particularly preferably at least 0.925 g/cm 3 and moreover preferably at least 0.930 g/cm 3 .
  • the layer of thermoplastic KSv is present as a mixture of at least two thermoplastics.
  • the layer of plastic KSv it is furthermore preferable for the layer of plastic KSv to comprise at least 25 wt.%, particularly preferably at least 35 wt.% and most preferably at least 45 wt.%, in each case based on the layer of plastic KSu, of a thermoplastic which has a Vicat softening temperature of at least 90 °C, preferably at least 95 °C and particularly preferably at least 100 °C.
  • This thermoplastic furthermore preferably has a melting point of at least 1 10 °C, preferably at least 1 15 °C and particularly preferably at least 120 °C.
  • This thermoplastic moreover preferably has a density of at least 0.918 g/cm 3 , preferably at least 0.922 g/cm , particularly preferably at least 0.925 g/cm and moreover preferably at least 0.930 g/cm 3 .
  • the layer of thermoplastic KSv prefferably has a Vicat softening temperature in a range of from 90 °C to 150 °C, preferably from 95 °C to 140 °C and particularly preferably from 100 °C to 135 °C.
  • the layer of plastic KSv is present as a mixture of a polyolefin prepared by means of a metallocene catalyst and a further polymer, the further polymer preferably being a polyolefin which has not been prepared by means of a metallocene catalyst, preferably a polyethylene which has not been prepared by means of a metallocene catalyst (mPE).
  • mPE metallocene catalyst
  • the layer of thermoplastic KSv is present as a mixture of 25 to 95 wt.%, preferably 35 to 85 wt.% and particularly preferably 45 to 75 wt.% of mPE and 5 to 75 wt.%, preferably 15 to 65 wt.% and particularly preferably 25 to 55 wt.% of PE, the mPE described here fulfilling at least one, preferably at least two and particularly preferably all of the parameters of Vicat softening temperature, melting temperature, MFR value and density mentioned above for the layer of thermoplastic KSv.
  • the layer of thermoplastic KSv is present as a mixture of at least two thermoplastics.
  • the layer of plastic KSv it is furthermore preferable for the layer of plastic KSv to comprise at least 25 wt.%, particularly preferably at least 35 wt.% and most preferably at least 45 wt.%, in each case based on the layer of plastic KSv, of a thermoplastic which has a Vicat softening temperature of at least 90 °C, preferably at least 95 °C and particularly preferably at least 100 °C.
  • This thermoplastic furthermore preferably has a melting point of at least 1 10 °C, preferably at least 115 °C and particularly preferably at least 120 °C.
  • This thermoplastic moreover preferably has a density of at least 0.918 g/cm 3 , preferably at least 0.922 g/cm 3 , particularly preferably at least 0.925 g/cm 3 and moreover preferably at least 0.930 g/cm 3 .
  • the barrier layer any material which is suitable for this purpose to the person skilled in the art and has an adequate barrier action, in particular against oxygen, can be employed.
  • the barrier layer is preferably chosen from
  • the barrier layer is a barrier layer of plastic according to alternative a., this preferably comprises at least 70 wt.%, particularly preferably at least 80 wt.% and most preferably at least 95 wt.% of at least one plastic which is known to the person skilled in the art for this purpose, in particular because of aroma or gas barrier properties which are suitable for packaging containers.
  • Possible plastics, in particular thermoplastics, here are plastics carrying N or O, both by themselves and in mixtures of two or more. According to the invention, it may prove advantageous if the barrier layer of plastic has a melting temperature in a range of from more than 155 to 300 °C, preferably in a range of from 160 to 280 °C and particularly preferably in a range of from 170 to 270 °C.
  • the barrier layer of plastic has a weight per unit area in a range of from 2 to 120 g/m 2 , preferably in a range of from 3 to 60 g/m 2 , particularly preferably in a range of from 4 to 40 g/m 2 and moreover preferably from 6 to 30 g/m 2 .
  • the barrier layer of plastic is obtainable from melts, for example by extrusion, in particular layer extrusion.
  • the barrier layer of plastic can also be introduced into the sheetlike composite via lamination. It is preferable here for a film to be incorporated into the sheetlike composite.
  • barrier layers of plastic which are obtainable by deposition from a solution or dispersion of plastics can also be chosen.
  • Possible suitable polymers are preferably those which have a weight-average molecular weight, determined by gel permeation chromatography (GPC) by means of light scattering, in a range of from 3xl0 3 to lxlO 7 g/mol, preferably in a range of from 5 l0 3 to lxlO 6 g/mol and particularly preferably in a range of from 6xl0 3 to lx lO 5 g/mol.
  • Possible suitable polymers are, in particular, polyamide (PA) or polyethylene/vinyl alcohol (EVOH) or a mixture thereof.
  • PA 6 PA 6.6, PA 6.10, PA 6.12, PA 1 1 or PA 12 or a mixture of at least two of these are to be mentioned here in particular, PA 6 and PA 6.6 being particularly preferred and PA 6 furthermore being preferred.
  • PA 6 is commercially obtainable, for example, under the trade names Akulon ® , Durethan ® and Ultramid ® .
  • the PA prefferably has a density in a range of from 1.01 to 1.40 g/cm 3 , preferably in a range of from 1.05 to 1.30 g/cm 3 and particularly preferably in a range of from 1.08 to 1.25 g/cm 3 . Furthermore, it is preferable for the PA to have a viscosity number in a range of from 130 to 185 ml/g and preferably in a range of from 140 to 180 ml/g.
  • EVOH all EVOHs which seem suitable for the use according to the invention to the person skilled in the art are possible.
  • EVALTM EVAL Europe NV, Belgium
  • EVALTM F104B EVALTM LR171B
  • Preferred EVOHs have at least one, two, several or all of the following properties:
  • a melting point in a range of from more than 155 to 235 °C, preferably from 165 to 225 °C;
  • an MFR value (210 °C/2.16 kg if T M( EVOH) ⁇ 230 °C; 230 °C/2.16 kg if 210 °C ⁇ TM ( EVOH) ⁇ 230 °C) in a range of from 1 to 25 g/10 min, preferably from 2 to 20 g/10 min;
  • an oxygen permeation rate in a range of from 0.05 to 3.2 cm 3 *20 ⁇ m/m 2 ⁇ day ⁇ atm, preferably in a range of from 0.1 to 1 cm « 20 ⁇ /m *dayatm.
  • the barrier layer is a metal layer. All layers with metals which are known to the person skilled in the art and can provide a high impermeability to light and oxygen are suitable in principle as the metal layer.
  • the metal layer can be present as a foil or as a deposited layer, e.g. formed by a physical gas phase deposition.
  • the metal layer is preferably an uninterrupted layer.
  • the metal layer has a thickness in a range of from 3 to 20 ⁇ , preferably a range of from 3.5 to 12 ⁇ and particularly preferably in a range of from 4 to ⁇ ⁇ .
  • Metals which are preferably chosen are aluminium, iron or copper.
  • a steel layer, e.g. in the form of a foil, may be preferred as an iron layer.
  • the metal layer is a layer with aluminium.
  • the aluminium layer can expediently be made of an aluminium alloy, such as, for example, AlFeMn, AlFel.5Mn, AlFeSi or AlFeSiMn.
  • the purity is conventionally 97.5 % and higher, preferably 98.5 % and higher, in each case based on the total aluminium layer.
  • the metal layer is made of an aluminium foil.
  • Suitable aluminium foils have an extensibility of more than 1 %, preferably of more than 1.3 % and particularly preferably of more than 1.5 %, and a tensile strength of more than 30 N/mm 2 , preferably more than 40 N/mm and particularly preferably more than 50 N/mm .
  • Suitable aluminium foils show a drop size of more than 3 mm, preferably more than 4 mm and particularly preferably of more than 5 mm in the pipette test.
  • Suitable alloys for establishing aluminium layers or foils are commercially obtainable under the designations EN AW 1200, EN AW 8079 or EN AW 81 1 1 from Hydro Aluminium GmbH or Amcor Flexibles Singen GmbH.
  • an adhesion promoter can be provided between the metal foil and the next layer of thermoplastic on one and/or both sides of the metal foil. According to a particular embodiment of the container according to the invention, however, an adhesion promoter is provided between the metal foil and the next layer of thermoplastic on no side of the metal foil.
  • a metal oxide layer can be chosen as the barrier layer according to alternative c.
  • Possible metal oxide layers are all metal oxide layers which are familiar and seem suitable to the person skilled in the art for achieving a barrier action against light, vapour and/or gas. Metal oxide layers based on the metals aluminium, iron or copper already mentioned above and those metal oxide layers based on titanium or silicon oxide compounds are preferred in particular.
  • a metal oxide layer is produced, by way of example, by vapour deposition of a metal oxide on a layer of plastic, for example an orientated polypropylene film. A preferred process for this is physical gas phase deposition.
  • the metal layer or the metal oxide layer can be present as a layer composite of one or more layers of plastic with a metal layer.
  • the sheetlike composite according to the invention has at least one further layer of thermoplastic KSa, the layer of thermoplastic KSa preferably lying between layer iii. and layer iv.
  • the layer of thermoplastic KSa follows the barrier layer, and preferably follows indirectly, for example via an adhesion promoter layer.
  • no further layer, in particular no adhesion promoter layer is provided between the barrier layer and the layer of thermoplastic KSa.
  • the layer of thermoplastic KSw preferably follows the layer of thermoplastic KSa, and particularly preferably follows directly. If the composite according to the invention has no layer of thermoplastic KSa, the layer of thermoplastic KSw follows the barrier layer, preferably indirectly, for example via an adhesion promoter layer. In another embodiment example, in the absence of the layer of thermoplastic KSa, also no further layer, in particular no adhesion promoter layer, is provided between the layer of thermoplastic KSw and the barrier layer.
  • the layer of thermoplastic KSa preferably has a weight per unit area in a range of from 5 to
  • the layer of thermoplastic KSa is in a range of from 90 °C to 150 °C, preferably from 95 °C to 140 °C and particularly preferably from 100 °C to 135 °C.
  • the layer of thermoplastic KSa is present as a mixture of at least two thermoplastics.
  • the layer of thermoplastic KSa it is furthermore preferable for the layer of thermoplastic KSa to comprise at least 25 wt.%, particularly preferably at least 35 wt.% and most preferably at least 45 wt.%, in each case based on the layer of thermoplastic KSa, of a thermoplastic which has a Vicat softening temperature of at least 90 °C, preferably at least 95 °C and particularly preferably at least 100 °C.
  • This thermoplastic furthermore preferably has a melting point of at least 1 10 °C, preferably at least 1 15 °C and particularly preferably at least 120 °C.
  • This thermoplastic moreover preferably has a density of at least 0.918 g/cm 3 , preferably at least 0.922 g/cm 3 , particularly preferably at least 0.925 g/cm 3 and moreover preferably at least 0.930 g/cm 3 .
  • the layer of thermoplastic KSa is present as a mixture of a polyolefin prepared by means of a metallocene catalyst and a further polymer, the further polymer preferably being a polyolefin which has not been prepared by means of a metallocene catalyst, preferably a polyethylene which has not been prepared by means of a metallocene catalyst.
  • the layer of thermoplastic KSa is present as a mixture of 25 to 95 wt.%, preferably 35 to 85 wt.% and particularly preferably 45 to 75 wt.% of mPE and 5 to 75 wt.%, preferably 15 to 65 wt.% and particularly preferably 25 to 55 wt.% of PE, the mPE described here fulfilling at least one, preferably at least two and particularly preferably all of the parameters of Vicat softening temperature, melting temperature, MFR value and density mentioned above for the layer of thermoplastic KSv.
  • thermoplastic KSw which preferably has a weight per unit area in a range of from 2 to 60 g/m 2 , particularly preferably from 5 to 50 g/m 2 and moreover preferably from 7 to 40 g/m 2 .
  • thermoplastics which seem suitable to the person skilled in the art can be used.
  • the layer of thermoplastic KSw occurs as a mixture of at least two thermoplastics.
  • the layer of thermoplastic KSw is based on a mixture of at least two polymers, one polymer preferably having a density in a range of from 0.910 to 0.930 g/cm 3 , preferably from 0.915 to 0.925 g/cm 3 . Furthermore preferably, this polymer has a melting temperature in a range of from 100 °C to 1 15 °C.
  • a second polymer preferably has a density in a range of from 0.880 to 0.915 g/cm 3 , preferably 0.890 to 0.910 g/cm 3 and particularly preferably additionally a melting temperature in a range of from 90 °C to 1 15 °C.
  • the layer KSw has a Vicat softening temperature in a range of from 60 to 105 °C, preferably from 65 to 100 °C and particularly preferably from 70 to 95 °C.
  • the layer of plastic KSw is present as a mixture of a polyolefin prepared by means of a metallocene catalyst and a further polymer, the further polymer preferably being a polyolefin which has not been prepared by means of a metallocene catalyst, preferably a polyethylene which has not been prepared by means of a metallocene catalyst.
  • the layer of plastic KSw is present as a mixture of 65 to 95 wt.%, preferably 70 to 90 wt.% and particularly preferably 75 to 85 wt.% of mPE and 5 to 35 wt.%, preferably 10 to 30 wt.% and particularly preferably 15 to 25 wt.% of PE.
  • the layer of thermoplastic KSw is present as a mixture of 15 to 45 wt.%, preferably 20 to 40 wt.% and particularly preferably 25 to 35 wt.% of mPE and 55 to 85 wt.%, preferably 60 to 80 wt.% and particularly preferably 65 to 75 wt.% of PE.
  • one or more or all of the layers of thermoplastic of the composite KSu, KSv, KSw and optionally KSa can also comprise an inorganic solid as a filler, in addition to a thermoplastic polymer.
  • the particular layer of thermoplastic it is preferable for the particular layer of thermoplastic to comprise a thermoplastic polymer or polymer mixture to the extent of at least 60 wt.%, preferably at least 80 wt.% and particularly preferably at least 95 wt.%, in each case based on the corresponding layer of thermoplastic.
  • All solids which seem suitable to the person skilled in the art are possible as the inorganic solid, preferably particulate solids, preferably metal salts or oxides of di- to tetravalent metals.
  • the average particle sizes (d50 %) of the inorganic solids, determined by sieve analysis, are preferably in a range of from 0.1 to 10 ⁇ , preferably in a range of from 0.5 to 5 ⁇ and particularly preferably in a range of from 1 to 3 ⁇ .
  • At least one, preferably at least two and furthermore preferably at least three of the layers of thermoplastic KSu, KSv, KSw and optionally KSa is a plastics mixture of at least two plastics.
  • at least one of the layers of thermoplastic KSu, KSv, KSw and optionally Sa is made of a polyethylene or a polypropylene or a mixture of at least two of these.
  • At least one of the layers of thermoplastic KSu, KSa, KSw and optionally KSa is present as a mixture of a polyolefin prepared by means of a metallocene catalyst and a further polymer, the further polymer preferably being a polyolefin which has not been prepared by means of a metallocene catalyst, preferably a polyethylene which has not been prepared by means of a metallocene catalyst (mPE).
  • mPE metallocene catalyst
  • the layer of thermoplastic KSv is present as a mixture of 25 to 95 wt.%, preferably 35 to 85 wt.% and particularly preferably 45 to 75 wt.% of mPE and 5 to 75 wt.%, preferably 15 to 65 wt.% and particularly preferably 25 to 55 wt.% of PE, the mPE described here fulfilling at least one, preferably at least two and particularly preferably all of the abovementioned parameters.
  • At least one of the layers of plastic KSu, KSv, KSw and optionally KSa contains at least one of the layers of plastic KSu, KSv, KSw and optionally KSa contains at
  • 3 least one polyolefin with a mass density in a range of from 0.918 g/cm to 0.980 g/cm , preferably from 0.922 to 0.970 g/cm , particularly preferably from 0.925 to 0.965 g/cm and moreover preferably from 0.930 to 0.960 g/cm 3 in a range of from 20 wt.% to 100 wt.%, preferably from 45 to 95 wt.% and particularly preferably from 65 to 85 wt.%, in each case based on the total weight of the layer of plastic.
  • the layers of plastic KSu, KSv and optionally KSa have, in particular, the abovementioned mass density.
  • the two layers of plastic KSv and KSu and moreover preferably the layers of plastic KSu, KSv and optionally KSa have a mass density in the abovementioned range.
  • the mass density of the layer of plastic KSw does not lie in the range mentioned.
  • the layers of thermoplastic KSu, KSv, KSw and optionally KSa each have a melting temperature in the range of from 80 to 155 °C.
  • the Vicat softening temperature of the layer of thermoplastic KSu is higher, particularly preferably by in each case at least 4 K, at least 6 K, at least 8 K, at least 10 K, at least 12 K, at least 14 K, at least 16 K or at least 18 K higher than the Vicat softening temperature of the layer of thermoplastic KSw.
  • the Vicat softening temperature of the layer of thermoplastic KSv is also higher, particularly preferably by in each case at least 4 K, at least 6 K, at least 8 K, at least 10 K, at least 12 K, at least 14 K, at least 16 K or at least 18 K higher than the Vicat softening temperature of the layer of thermoplastic KSw.
  • the Vicat softening temperature of the at least one layer of thermoplastic KSu, and particularly preferably also of the layer of thermoplastic KSv is in each case in a range of from 85 to 140 °C, or from 90 to 135 °C or from 95 to 130 °C.
  • the Vicat softening temperature of the at least one layer of plastic KSw is preferably in a range of from 60 °C to 105 °C, or from 65 °C to 100 °C or from 70 °C to 95 °C.
  • the melting temperature of the layer of thermoplastic KSu is higher, particularly preferably by in each case at least 3 K, or 4 K, at least 6 K, at least 8 K, at least 10 K, at least 12 K, at least 14 K, at least 16 K or at least 18 K higher than the melting temperature of the layer of thermoplastic KSw.
  • the melting temperature of the layer of thermoplastic KSv is likewise higher, particularly preferably by in each case at least 3 K, or 4 K, at least 6 K, at least 8 K, at least 10 K, at least 12 K, at least 14 K, at least 16 K or at least 18 K higher than the melting temperature of the layer of thermoplastic KSw. Maximum differences in the melting temperatures of 60 K are often observed.
  • the melting temperature of the layer of thermoplastic KSu, and optionally of the layer of thermoplastic KSv is in each case in a range of from 100 to 150 °C, or from 105 to 140 °C.
  • the melting temperature of the layer of thermoplastic KSw is preferably in a range of from 80 °C to 120 °C, or from 85 °C to 1 15 °C, or from 90 °C to 1 10 °C. It is furthermore preferable for the particular layer of thermoplastic furthest removed from the carrier layer - often called a layer of thermoplastic KSw - to be present as a mixture of at least two plastics.
  • no metal foil is provided between the carrier layer and the layer of thermoplastic KSw.
  • adhesion promoters in the adhesion promoter layer are all plastics which, due to functionalization by means of suitable functional groups, are suitable for generating a firm join by the formation of ionic bonds or covalent bonds to the surface of the other particular layer.
  • these are functionalized polyolefins which have been obtained by copolymerization of ethylene with acrylic acids, such as acrylic acid, methacrylic acid, crotonic acid, acrylates, acrylate derivatives or carboxylic acid anhydrides carrying double bonds, for example maleic anhydride, or at least two of these.
  • EEMAH polyethylene-maleic anhydride graft polymers
  • EAA ethylene/acrylic acid copolymers
  • EMA ethylene/methacrylic acid copolymers
  • the adhesion between the carrier layer, the layer of thermoplastic KSu or KSv, preferably at least two of these, the particular next layer to be at least 0.5 N/15 mm, preferably at least 0.7 N/15 mm and particularly preferably at least 0.8 N/ 15 mm.
  • the adhesion between the layer of thermoplastic KSu and the carrier layer to be at least 0.3 N/15 mm, preferably at least 0.5 N/15 mm and particularly preferably at least 0.7 N/15 mm.
  • the adhesion between the barrier layer and the layers adjacent to the barrier layer in the case of directly following layers of thermoplastic KSv and/or KSa prefferably at least 0.8 N/15 mm, preferably at least 1.0 N/15 mm and particularly preferably at least 1.4 N/15 mm.
  • the adhesion between the barrier layer and the adhesion promoter layer it is preferable for the adhesion between the barrier layer and the adhesion promoter layer to be at least 1.8 N/15 mm, preferably at least 2.2 N/15 mm and particularly preferably at least 2.8 N/15 mm.
  • the adhesion between the individual layers is so strongly formed that in the adhesion test tearing of the carrier layer, and in the case of a cardboard as the carrier layer, a so-called tearing of the cardboard fibre, occurs.
  • the carrier layer can have at least one hole.
  • the hole is covered at least with the barrier layer and at least the layer of thermoplastic KSw as a hole-covering layer.
  • the carrier layer of the composite has a hole which is covered at least with the layer of thermoplastic KSv, the barrier layer and the layers of thermoplastic KSw and optionally the layer of thermoplastic KSa as hole-covering layers. It is particularly preferable for the hole additionally to be covered with the layer of thermoplastic KSu.
  • One or more further layers, in particular adhesion promoter layers, can furthermore be provided between the layers already mentioned. It is preferable here for the hole-covering layers to be joined to one another at least partly, preferably to the extent of at least 30 %, preferably at least 70 % and particularly preferably to the extent of at least 90 % of the area formed by the hole.
  • the hole it is preferable for the hole to penetrate through the entire composite and to be covered by a closure or opening device which closes the hole.
  • the hole provided in the carrier layer can have any form which is known to the person skilled in the art and is suitable for various closures, drinking straws or opening aids.
  • the opening of such a container is usually generated by at least partial destruction of the hole- covering layers covering the hole. This destruction can be effected by cutting, pressing into the container or pulling out of the container. The destruction can be effected by an openable closure joined to the container and arranged in the region of the hole, usually above the hole, or a drinking straw which is pushed through the hole-covering layers covering the hole.
  • the carrier layer of the composite has a plurality of holes in the form of a perforation, the individual holes being covered at least with the barrier layer and the layer of thermoplastic KSw as the hole-covering layer.
  • a container produced from such a composite can then be opened by tearing along the perforation.
  • Such holes for perforations are preferably generated by means of a laser.
  • the use of laser beams is particularly preferred if a metal foil or a metallized foil is employed as the barrier layer.
  • the perforation to be introduced by mechanical perforation tools, usually having blades.
  • the sheetlike composite is subjected to a heat treatment at least in the region of the at least one hole.
  • this heat treatment also to be carried out around the edge region of the hole.
  • the heat treatment can be carried out by radiation, by hot gas, by thermal contact with a solid, by mechanical vibrations or by a combination of at least two of these measures.
  • the heat treatment is carried out by irradiation, preferably electromagnetic radiation and particularly preferably electromagnetic induction or also by hot gas.
  • irradiation preferably electromagnetic radiation and particularly preferably electromagnetic induction or also by hot gas.
  • the plastics of the layers of thermoplastic of the sheetlike composite contain no comonomers which are known to the person skilled in the art to have the effect of an improvement in adhesion, usually by the formation of chemical bonds.
  • Such comonomers are mentioned inter alia in the abovementioned adhesion promoter layers.
  • the layers of thermoplastic KSv and optionally KSa are therefore as a rule not suitable as adhesion promoters or as adhesive layers.
  • the present invention also provides a process for the production of the sheetlike composite described above. All the processes which are known to the person skilled in the art and seem suitable for the production of the composite according to the invention are possible for this.
  • the sheetlike composite according to the invention can be produced by a process which comprises, inter alia, the following process steps:
  • thermoplastic application of at least one further layer of thermoplastic to the opposite side of the composite precursor.
  • a composite precursor comprising at least the carrier layer is first produced.
  • the composite precursor preferably comprises the carrier layer, which can already have one or more holes and to which optionally at least one printed layer is applied.
  • this composite precursor is a non-printed carrier layer.
  • step B at least one layer of thermoplastic is applied to the composite precursor provided.
  • the application of this at least one layer is preferably carried out by melt coating, preferably by extrusion coating.
  • melt coating preferably by extrusion coating.
  • layers of thermoplastic, barrier layers and/or adhesion promoter layers to be applied sequentially or simultaneously by coextrusion in step B.
  • step C at least one further layer of thermoplastic is then applied to the opposite side of the composite precursor.
  • the application of this at least one further layer of thermoplastic is preferably carried out by melt coating, preferably by extrusion coating.
  • melt coating preferably by extrusion coating.
  • layers of thermoplastic, barrier layers and/or adhesion promoter layers to be applied sequentially or simultaneously by coextrusion in step C.
  • the at least one film or a multilayer composite film is provided in the form of a roll and is laminated on to the composite via further layers, preferably layers of thermoplastic or adhesion promoter layers. This is the case in particular during introduction of metal layers, in particular of metal foils.
  • the sheetlike composite has one or more holes to facilitate ease of opening, these can be introduced into the sheetlike composite either before step A., after step B. or after step C.
  • a non-printed carrier layer which already has holes is provided as the composite precursor in step A.
  • step B the layer of thermoplastic KSu is then first applied to the composite precursor.
  • step C the layer of thermoplastic KSv, the barrier layer, the layer of thermoplastic KSw and optionally the layer of thermoplastic KSa are then applied.
  • one or more adhesion promoter layers can also be co-applied here.
  • step B first the layer of thermoplastic KSv, the barrier layer, the layer of thermoplastic KSw and optionally the layer of thermoplastic KSa are applied.
  • step C the layer of thermoplastic KSu is then applied.
  • each case further layers for example adhesion promoter layers, can be co-applied.
  • the extrusion can be carried out in individual layers by a series of successive individual extruders or also in multiple layers by coextrusion, the abovementioned sequence of the individual layers always being retained.
  • a combination of extrusion and lamination coating can also take place in the process according to the invention.
  • At least one of the two In connection with the sheetlike composite, but also in connection with the composite precursor, it is preferable for at least one of the two to have at least one or two and more scores along which edges are formed during production of the container. This facilitates the folding and the formation of a kink running along the line prepared by the score, in order to achieve in this way a fold which is as uniform and accurately positioned as possible.
  • the scores can be introduced already before step A, after step B or also after step C, it being preferable for the scoring to be carried out after step C, that is to say after the coating of the both sides of the carrier layer.
  • the sheetlike composite is produced, usually as roll goods, by coextrusion of the individual layers of the sheetlike composite.
  • the scores are provided on these roll goods.
  • the scores it is also possible for the scores to be produced in the carrier layer already before the coating.
  • the carrier layer includes a hole or several holes, for at least one of the layers of thermoplastic KSu, KSv, KSw or optionally KSa to be stretched during the application, this stretching preferably being carried out by melt stretching, very particularly preferably by monoaxial melt stretching.
  • the layer is applied in the molten state to the composite precursor by means of a melt extruder and the layer applied, which is still in the molten state, is then stretched in preferably the monoaxial direction in order to achieve an orientation of the polymer in this direction.
  • the layer applied is then allowed to cool for the purpose of thermofixing.
  • the stretching is particularly preferable for the stretching to be carried out by at least the following application steps: bl . emergence of the at least one layer of thermoplastic as at least one melt film via at least one extruder die slot with an exit speed V ex ; t ; b2.
  • V ex i t ⁇ V a d v - It is particularly preferable for V a dv to be greater than V ex i t by a factor in the range of from 5 to 200, particularly preferably in a range of from 7 to 150, moreover preferably in a range of from 10 to 50 and most preferably in a range of from 15 to 35. In this context, it is preferable for V a d v to be at least 100 m/min, particularly preferably at least 200 m/min and very particularly preferably at least 350 m/min, but not to lie above 1 ,300 m/min.
  • the melt layer After the melt layer has been applied to the composite precursor by means of the stretching process described above, the melt layer is allowed to cool for the purpose of thermofixing, this cooling preferably being carried out by quenching via contact with a surface which is kept at a temperature in a range of from 5 to 50 °C, particularly preferably in a range of from 10 to 30 °C.
  • thermofixing it may prove to be particularly advantageous if the sheetlike composite is heat-treated at least in the region of the at least one hole, in order to effect there an at least partial elimination of the orientation of the polymer.
  • thermoplastic KSu, KSv, KSw or optionally KSa is produced by extrusion or coextrusion of at least one polymer PI through a slot die to obtain an emerging surface, at least one polymer P2 which differs from polymer PI being provided on the flanks of the surface of the at least one polymer PI emerging from the slot die.
  • Thermoplastic polymers are preferably chosen as the polymer P2.
  • Preferred thermoplastic polymers have a high rate of branching, a wide molecular weight distribution, and in the case of extrusion coating, after exit from the die have a low tendency towards "neck-in” and "edge-waving" or film striking.
  • thermoplastic to be employed depends on which of the layers of thermoplastic KSu, KSv, KSw or optionally KSa is to be produced by extrusion or coextrusion.
  • suitable and preferred thermoplastics reference is made to the description of the layers of plastic KSu, KSv, KSw and optionally KSa.
  • the thermoplastic chosen or the mixture of thermoplastics chosen then form PI of the particular layer of thermoplastic. During a coextrusion of different layers, the surface F is formed from several different thermoplastics or plastics mixtures PI .
  • the polymer P2 can likewise also be a constituent of the surface F.
  • One or more thermoplastics preferably polyethylenes, particularly preferably LDPE and moreover preferably LDPE prepared in an autoclave reactor, are particularly suitable as polymer P2.
  • suitable polymers are 23L430 or 19N430 from Ineos. It is also conceivable for a mixture of at least two suitable polymers to be employed as the edge layer P2.
  • the polymer PI and the polymer P2 are preferably coextruded. They thus form intimately bonded regions of the emerging surface.
  • the polymer stream P2 can be fed to the extruder die. If the P2 is also a constituent of the film F, this can be branched off into a separate polymer stream in the feed block and passed to the edge region of the extruder die. Alternatively, an additional extruder which provides the P2 and leads it to the extruder die can also be provided.
  • thermoplastics are conventionally heated to temperatures of from 210 to 330 °C, measured on the molten polymer film below the exit at the extruder die.
  • the extrusion can be carried out by means of extrusion tools which are known to the person skilled in the art and commercially obtainable, such as, for example, extruders, extruder screws, feed block etc.
  • the area which has emerged is cooled to a temperature below the lowest melting temperature of the polymers P 1 and P2 provided in this surface or in its flanks, and at least the flanks of this surface are then separated off from this surface. Cooling can be carried out in any manner which is familiar to the person skilled in the art and seems to be suitable. The thermofixing already described above is also preferred here. At least the flanks are then separated off from the surface F.
  • the separating off can be carried out in any manner which is familiar to the person skilled in the art and seems to be suitable.
  • the separating off is carried out by a knife, laser beam or water jet, or a combination of two or more of these, the use of knives, in particular knives for a shear cut, being particularly preferred.
  • the present invention also provides a container which surrounds an interior and comprises at least the sheetlike composite described above.
  • the embodiments, and in particular the preferred embodiments, described in connection with the sheetlike composite according to the invention are also preferred for the container according to the invention.
  • the present invention also provides a container which surrounds an interior and comprises at least the sheetlike composite described above.
  • the embodiments, and in particular the preferred embodiments, described in connection with the sheetlike composite according to the invention are also preferred for the container according to the invention.
  • the present invention also provides a process for the production of a container surrounding an interior, including at least the steps a. provision of a sheetlike composite comprising a layer configuration with at least the following 5 layers:
  • thermoplastic KSu of a plastics composition KSum i. a first layer of thermoplastic KSu of a plastics composition KSum; ii. a carrier layer;
  • thermoplastic KSw of a plastics composition KSwm; wherein layers i. to iv. preferably occur in the sequence shown;
  • the sheetlike composite has at least one further layer of thermoplastic KSv from a plastics composition KSvm, wherein the layer of thermoplastic KSv preferably lies between layer ii. and layer iv.;
  • the Vicat softening temperature of the plastics composition KSum is higher than the Vicat softening temperature of the plastics composition KSwm;
  • the plastics compositions employed according to the invention can be made of a single thermoplastic or from two or more thermoplastics. The above statements therefore apply here accordingly to the thermoplastics and the layers of thermoplastic.
  • the plastics compositions can be fed to an extruder in any form which is suitable for extruding to the person skilled in the art.
  • the plastics compositions are employed as powders or granules, preferably as granules.
  • the embodiments, and in particular the preferred embodiments, described in connection with the sheetlike composite according to the invention are also preferred in the process according to the invention for the production of the container surrounding an interior. It is preferable in particular for the Vicat softening temperature of the plastics composition KSum also to be higher than the Vicat softening temperature of the plastics composition KSwm. In a further embodiment example of the process according to the invention, it is preferable for the Vicat softening temperature of the plastics composition KSvm also to be higher than the Vicat softening temperature of the plastics composition KSwm.
  • the Vicat softening temperature of the plastics composition KSum is higher, particularly preferably by in each case at least 4 K, at least 6 K, at least 8 K, at least 10 K, at least 12 K, at least 14 K, at least 16 K or at least 18 K, than the Vicat softening temperature of the plastics composition KSwm.
  • the Vicat softening temperature of the plastics composition KSvm is also higher, particularly preferably by in each case at least 4 K, at least 6 K, at least 8 K, at least 10 K, at least 12 K, at least 14 K, at least 16 K or at least 18 K, than the Vicat softening temperature of the plastics composition KSwm. Maximum differences in the Vicat softening temperatures of 60 K are often observed.
  • step a If the roll goods provided with scores are not employed directly in step a., container blanks for an individual container are obtained from the roll goods and are provided as the sheetlike composite in step a.
  • the container according to the invention can have a large number of different forms, but an essentially square-shaped structure is preferred.
  • the container can furthermore be formed over its complete surface from the sheetlike composite, or can have a 2- or multi-part structure.
  • other materials can also be employed, for example plastic material, which can be employed in particular in the top or the base regions of the container.
  • the container it is preferable here for the container to be constructed from the sheetlike composite to the extent of at least 50 %, particularly preferably to the extent of at least 70 % and moreover preferably to the extent of at least 90 % of the surface.
  • the container can have a device for emptying the contents.
  • the container according to the invention has at least one, preferably from 4 to 22 or also more edges, particularly preferably from 7 to 12 edges.
  • edge is understood as meaning regions which are formed on folding a surface. Edges which may be mentioned by way of example are the elongated contact regions of in each case two wall surfaces of the container.
  • the container walls preferably represent the surfaces of the container framed by the edges.
  • process step a. of the process according to the invention a sheetlike composite obtained by the process described above for the production of a sheetlike composite is first provided, from which a container precursor is then formed by folding in process step b.
  • the at least one, preferably at least two of the layers of thermoplastic KSu, KSv, KSw and optionally KSa, further preferably at least the layer of plastic KSw, and particularly preferably each of the layers of thermoplastic KSu, KSv, KSw and optionally KSa, has a temperature above the melting temperature of the particular layer.
  • step b the at least one, preferably at least two of the layers of thermoplastic KSu, KSv, KSw and optionally KSa, further preferably at least the layer of thermoplastic KSw, and particularly preferably each of the layers of thermoplastic KSu, KSv, KSw and optionally KSa, has a temperature below the melting temperature of the particular layer.
  • At least one, preferably at least two of the layers of thermoplastic KSu, KSv, KSw and optionally KSa, further preferably at least the layers of thermoplastic KSw and optionally KSa, or also all of the layers of thermoplastic KSu, KSv, KSw and optionally KSa has or have a melting temperature below the melting temperature of the barrier layer.
  • the melting temperatures of the at least one, preferably of the at least two of the layers of thermoplastic KSu, KSv, KSw and optionally KSa, further preferably at least of the layers of thermoplastic KSw and optionally KSa or also of all the layers of thermoplastic KSu, KSv, KSw and optionally KSa and the melting temperature of the barrier layer preferably differ here by at least 1 K, particularly preferably by at least 10 K, still more preferably by at least 50 K, moreover preferably at least 100 K.
  • the temperature difference should preferably be chosen only high enough so that no melting of the barrier layer, in particular no melting of the barrier layer of plastic, occurs during the folding.
  • a further folding follows step d.
  • step e in the further folding at least one, preferably each of the layers of thermoplastic KSu, KSv, KSw and optionally KSa having a temperature which is below the melting temperature of this layer of thermoplastic.
  • folding is understood as meaning an operation in which preferably an elongated kink forming an angle is generated in the folded sheetlike composite by means of a folding edge of a folding tool. For this, two adjacent surfaces of a sheetlike composite are often bent ever more towards one another. By the fold, at least two adjacent fold surfaces are formed, which can then be joined at least in part regions to form a container region.
  • the joining can be effected by any measure which appears to be suitable to the person skilled in the art and which makes possible a join which is as gas- and liquid-tight as possible.
  • the joining can be carried out by sealing or gluing or a combination of the two measures.
  • sealing the join is created by means of a liquid and solidification thereof.
  • gluing chemical bonds which create the join form between the interfaces or surfaces of the two objects to be joined.
  • sealing or gluing it is often advantageous for the surfaces to be sealed or glued to be pressed together with one another.
  • the sealing temperature is preferably chosen such that the thermoplastics involved in the sealing, preferably the polymers of the layer of thermoplastic KSu and/or of the layer of thermoplastic KSw, are present as a melt.
  • the sealing temperatures are therefore at least 1 K, preferably at least 5 and particularly preferably at least 10 K above the melting temperature of the particular plastic.
  • the sealing temperature chosen should not be too high, in order that the exposure of the plastic or plastics to heat is not unnecessarily severe, so that they do not lose their envisaged material properties.
  • the container is filled with a foodstuff before step b. or after step c.
  • foodstuffs known to the person skilled in the art for human consumption and also animal feeds are possible as the foodstuff.
  • Preferred foodstuffs are liquid above 5 °C, for example dairy products, soups, sauces and non-carbonated drinks. The filling can be carried out in various ways.
  • the foodstuff and the container can be sterilized separately, before the filling, to the greatest degree possible by suitable measures such as treatment of the container with H 2 0 2 , UV radiation or other suitable high-energy radiation, plasma treatment or a combination of at least two of these, as well as heating of the foodstuff, and the container is then filled.
  • This type of filling is often called "aseptic filling" and is preferred according to the invention.
  • it is furthermore a widespread procedure to heat the container filled with foodstuff to reduce the germ count. This is preferably carried out by pasteurization or autoclaving. Less sterile foodstuffs and containers can also be employed in this procedure.
  • a tubular structure with a fixed longitudinal seam first to be formed from the sheetlike composite by sealing or gluing the overlapping borders.
  • This tubular structure is compressed laterally, fixed and separated and formed into an open container by folding and sealing or gluing.
  • the foodstuff here can already be filled into the container before the fixing and before the separation and folding of the base in the sense of step b.
  • a container which is obtained by shaping the sheetlike composite and is opened on one side to be employed.
  • Shaping of the sheetlike composite and obtaining of such an opened container can be carried out by steps b. and c. by any procedure which appears to be suitable for this to the person skilled in the art.
  • shaping can be carried out by a procedure in which sheet-like container blanks which already take into account the shape of the container in their cut-out are folded such that an opened container precursor is formed. This is as a rule effected by a procedure in which after folding of this container blank, its longitudinal edges are sealed or glued to form a side wall and the one side of the container precursor is closed by folding and further fixing, in particular sealing or gluing.
  • the fold surfaces it is preferable for the fold surfaces to form an angle ⁇ of less than 90°, preferably of less than 45° and particularly preferably of less than 20°.
  • the fold surfaces are often folded to the extent that these come to lie on one another at the end of the folding. This is advantageous in particular if the fold surfaces lying on one another are subsequently joined to one another in order to form the container base and the container top, which is often configured gable-like or also flat.
  • gable configuration reference may be made by way of example to WO 90/09926 A2.
  • At least one of the at least two layers of thermoplastic KSu and KSw, or also both is or are heated above the melting temperature of the layers of thermoplastic before step c.
  • heating is carried out to temperatures which are at least 1 K, preferably at least 5 K and particularly preferably at least 10 K above the melting temperature of these layers.
  • the temperature should as far as possible be above the melting temperature of the particular plastic to the extent that by the cooling, due to the folding, moving and pressing, the plastic does not cool to the extent that this becomes solid again.
  • the heating to these temperatures is carried out by irradiation, by mechanical vibrations, by contact with a hot solid or hot gas, preferably hot air, or a combination of these measures.
  • a hot solid or hot gas preferably hot air
  • any type of radiation which is suitable for softening the plastics to the person skilled in the art is possible.
  • Preferred types of radiation are IR rays, UV rays, microwaves or also electromagnetic radiation, in particular electromagnetic induction.
  • Preferred types of vibration are ultrasound.
  • the maximum transmission intensity of at least one of the perforated covering layers comprising a stretched polymer is furthermore preferable for the maximum transmission intensity of at least one of the perforated covering layers comprising a stretched polymer to differ before and after the heat treatment.
  • This can conventionally be ascertained by different representations of the region viewed through a polarization filter.
  • the heat-treated regions thus differ by light-dark contrasts from the regions on a surface which are adjacent to these but have not been heat-treated.
  • a difference in gloss is generally to be detected due to the change in structure of the polymer inner layer originating from the heat treatment, compared with the regions which have not been heat-treated. The same applies to regions before and after the heat treatment.
  • regions of the sheetlike composite can also be heat-treated. These also show a different maximum transmission intensity compared with the non-treated regions. These include all regions in which joining by sealing is carried out and/or scores for folding are provided. Among these regions, the longitudinal seams at which the sheetlike composite is formed into a tubular or jacket-like structure are particularly preferred. After the above heat treatment, the heat-treated regions can be allowed to cool again. According to the above embodiment, the invention also provides the use of the sheetlike composite according to the invention or of a container produced therefrom or comprising this composite for storage of foodstuffs, in particular of sterilized foodstuffs. Test methods:
  • the melting temperature with the aid of the DSC method: ISO 1 1357-1 , -5; if the sample is based on a mixture of several plastics and the determination of the melting temperature by the abovementioned method gives several peak temperatures T p , the highest of the peak temperatures T p>m which is to be assigned to a plastic of the plastics mixture is defined as the melting temperature.
  • the equipment is calibrated according to the manufacturer's instructions with the aid of the following measurements:
  • Pipette test In this, at least 10 drops of 5 ⁇ each of distilled water are applied to the surface to be tested and the drop size is determined.
  • the layer to be investigated is separated from the remaining layers by mechanical or chemical means. It is essential to ensure here that no contamination of the samples by adjacent layers occurs. From the sample material collected in this way, a test specimen can be established according to the dimensions stated in ISO 306:2004 and the Vicat softening temperature can be determined in accordance with the standard mentioned. If the material of plastic to be investigated is present as flocks or crumbs, these are processed to give a homogeneous test specimen. This can be carried out by pressing, careful heating or both measures.
  • the sheetlike composites were produced with the aid of the coating process described above by process steps A-C.
  • a carrier layer which optionally has holes for closures or drinking straws is first taken. This is first coated according to process step A with the layer of plastic KSu, and in process step C first the layer of plastic KSv, the adhesion promoter layer and then the barrier layer, followed by an adhesion promoter layer of the layer of plastic KSa and finally the layer of plastic KSw are then applied to the side of the carrier layer facing away from the layer of plastic KSu. This is as a rule carried out in a commercially available coating installation.
  • Example 2 the procedure is as in Example 1. There is merely the difference that first the barrier layer, the adhesion promoter layer and layer of plastic KSv are applied to the carrier layer on the side opposite the layer of plastic KSu, and the layer of plastic KSw is then applied.
  • 5b a schematic illustration along a section A-A in the folded state
  • 6 a schematic illustration of a sheetlike composite which can be employed in the process according to the invention
  • Figure 1 shows a container 2 surrounding an interior 1 and made of a sheetlike composite 3.
  • the container 2 is shown with the container upper side 12 facing upwards.
  • the container 2 is made of the sheetlike composite 3 which includes at least the carrier layer 4.
  • the container 2 can furthermore include a hole 36.
  • FIG. 2 shows a schematic flow of devices and production steps by the process according to the invention.
  • the sheetlike composite 3 is thus produced from a carrier layer 4, a barrier layer 5 and the layers of thermoplastic KSv 35, KSu 13 and KSw 7 and optionally a further layer of thermoplastic KSa 6 and - if necessary - at least one adhesion promoter layer 19 by an extrusion process and is usually provided as roll goods.
  • the score 14 is produced in the roll goods, which can have been provided with an imprint or decoration beforehand. Furthermore, if the roll goods provided with scores 14 are not employed as such for the production of containers, container blanks are produced in the composite fabrication 21.
  • FIG. 3 shows a container 2 formed during the process according to the invention, which - for a better view - is shown with a container region 23 envisaged for a base 12 on the top.
  • the container region 23 envisaged for the base 12 has a plurality of scores 14.
  • Figure 4a shows the cross-section through a sheetlike composite 3 with a score 14, formed by a recess 24 and a bulge 25.
  • FIG. 4b An edge 17 of a folding tool 18 is provided above the recess 24, in order to engage in the recess 24, so that folding can be carried out around the edge 17 along the score 14, in order to obtain a fold 8 shown as a cross-section in Figure 4b.
  • This fold 8 has two fold surfaces 9 and 10 which enclose an angle ⁇ and are present as a part 15 of large area and a part 16 of small area. At least one layer of thermoplastic 6, 7 or 13 is melted in a part region 1 1 of the part 16 of small area. By pressing the fold surfaces 9, 10 together, reducing the angle ⁇ to 0, the two fold surfaces 9, 10 are joined to one another by sealing.
  • Figure 5a shows a section along the line A-A in Figure 3, before folding, from a sheetlike composite 3 with scores 14.
  • edges 17 of folding tools 18 which engage in the scores 14 installed centrally on the front faces, the scores 14 are moved in the direction of the two arrows, as a result of which the folds 8 shown in Figure 5b with the angles ⁇ are formed.
  • the section shown here through the outermost part to be folded of the container region envisaged for the base 12 of the container 2 has a part region 1 1 towards the interior 1 in which at least one layer of thermoplastic 6, 7 or 13 is melted.
  • Figure 6 shows a sheetlike composite 3, the upper side lying on the outside of the container 2 produced therefrom and the under-side on the inside.
  • layer of thermoplastic KSu 13 usually PE optionally with a filler content of an inorganic salt
  • a carrier layer 4 of cardboard with a weight per unit area in a range of from 120 to 400 g/m 2
  • a layer of thermoplastic KSv 35 usually with a weight per unit area in a range of from 5 to 50 g/m 2
  • a barrier layer 5 for example a barrier of plastic
  • a weight per unit area in a range of from 2 to 120 g/m 2 followed by a layer of adhesion promoter 19 with a weight per unit area in a range of from 2 to 30 g/m 2
  • a layer of thermoplastic KSa 6 usually of PE
  • the sheetlike composite from Figure 6 is supplemented by a further layer 19 of adhesion promoter with a weight per unit area in a range of from 2 to 30 g/m 2 provided between the barrier layer 5, for example of a metal layer with a thickness of 3-12 ⁇ , and the carrier layer 4.
  • Figure 8a shows a folded composite region 30 of the sheetlike composite 3 between a sonotrode 28 and an anvil 34, both of which each have a surface relief 29.
  • the folded composite region is formed by further reduction of the angle ⁇ in the context of the folding shown in Figure 5b and often has an intermediate space 33 in the regions with few layers.
  • the surface relief 29 is configured such that recesses 33 in the surface relief 29 are opposite the multilayer regions 31 of greater thickness formed during folding, in order to allow a distribution of pressure and mechanical vibration over the sonotrode 28 which is as uniform as possible. Furthermore, the fixing of the folded composite region 30 to be joined, until the intermediate space 33 disappears, is improved in this way.
  • FIG. 8b shows the folded composite region, as shown in Fig. 8b, is pressed together and held according to the surface relief, so that the mechanical ultrasound vibration generated by the sonotrode 28 is transmitted to the folded composite 30 and joining by sealing takes place, in that the molten layers of plastic at least partly flow into one another due to the pressing pressure and solidify again by cooling, usually in a holding time, before the sonotrode 28 has released the folded composite region 30 treated in this way.
  • Figure 9 shows the coating process preferred according to the invention schematically a. in the front view and b. in the side view.
  • the coating film in the molten state 39 exits the extruder die slot 38 of an extruder die 37 and is applied to the carrier layer 4 via the cooling and pressing rolls 41.
  • the coating film forms the surface F which comprises the polymers PI 42 and P2 43, the polymer P2 43 forming the edge regions of the surface F.
  • the edge surfaces P2 43 of the surface F are preferably separated off from the surface F by cutting tools 44, preferably shearing blades.
  • the molten coating film 39 exits the extruder die 37 with the speed V ex i t and is accelerated to the speed V a dv by the cooling and pressing rolls and thus stretched monoaxially.
EP12740891.2A 2011-07-26 2012-07-23 Flächenförmiger verbund mit kunststoffschichten unterschiedlicher vicat-erweichungstemperaturen Active EP2736716B1 (de)

Priority Applications (1)

Application Number Priority Date Filing Date Title
PL12740891T PL2736716T3 (pl) 2011-07-26 2012-07-23 Płaski kompozyt z warstwami z tworzywa sztucznego o różnych temperaturach mięknienia vicata

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102011108402A DE102011108402A1 (de) 2011-07-26 2011-07-26 Flächenförmiger verbund mit kunststoffschichten unterschiedlicher vicat-erweichungstemperaturen
PCT/EP2012/003094 WO2013013801A1 (en) 2011-07-26 2012-07-23 Planar composite with layers of plastic of different vicat softening temperatures

Publications (2)

Publication Number Publication Date
EP2736716A1 true EP2736716A1 (de) 2014-06-04
EP2736716B1 EP2736716B1 (de) 2019-02-06

Family

ID=46598450

Family Applications (1)

Application Number Title Priority Date Filing Date
EP12740891.2A Active EP2736716B1 (de) 2011-07-26 2012-07-23 Flächenförmiger verbund mit kunststoffschichten unterschiedlicher vicat-erweichungstemperaturen

Country Status (12)

Country Link
US (1) US9902524B2 (de)
EP (1) EP2736716B1 (de)
CN (1) CN103702830B (de)
BR (1) BR112014001723B1 (de)
DE (1) DE102011108402A1 (de)
ES (1) ES2717897T3 (de)
IN (1) IN2014DN00225A (de)
MX (1) MX2014000982A (de)
PL (1) PL2736716T3 (de)
RU (1) RU2623265C2 (de)
TR (1) TR201905854T4 (de)
WO (1) WO2013013801A1 (de)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102014009466A1 (de) * 2014-06-30 2015-12-31 Sig Technology Ag Flächenförmiger Verbund mit einer mPolyolefinschicht mit verringertem Antioxidansanteil, insbesondere für Nahrungsmittelverpackungen
DE102014015958A1 (de) 2014-10-31 2016-05-04 Sig Technology Ag Vorrichtung, insbesondere zum Verschließen eines Kopfbereichs eines Nahrungsmittel-behälters, aus einem Laminat mit geschältem und umgeschlagenen Randbereich
US20160288949A1 (en) * 2015-03-31 2016-10-06 Steven Weymer Eco-carton
DE102015010405A1 (de) * 2015-08-14 2017-02-16 Sig Technology Ag Flächenförmiger Verbund, insbesondere für formstabile Behälter, mit teilflächig aufgebrachter äußerer thermoplastischer Siegelschicht
DE102015010404A1 (de) * 2015-08-14 2017-03-09 Sig Technology Ag Flächenförmiger Verbund, insbesondere für formstabile Behälter, mit teilflächig aufgebrachter äußerer thermoplastischer Siegelschicht, insbesondere zum Siegeln einer Längsnaht
EP3334609A1 (de) * 2015-08-14 2018-06-20 SIG Technology AG Elektrostatisch unterstütztes drucken eines verpackungslaminats für dimensionsstabile lebensmittelbehälter mit dem gefalteten verpackungslaminat
BR112018013116A2 (pt) * 2015-12-28 2018-12-11 Sig Technology Ag compósito em forma de folha, precursor de recipiente, processo e uso do compósito em forma de folha
DE102016209350A1 (de) * 2016-05-30 2017-11-30 Sig Technology Ag Elektrostatisch unterstütztes Bedrucken eines Packstofflaminats für formstabile Nahrungsmittelbehälter mit einer Vielzahl von Druckwerken
DE102016209351A1 (de) * 2016-05-30 2017-11-30 Sig Technology Ag Elektrostatisch unterstütztes Bedrucken eines Packstofflaminats für formstabile Nahrungsmittelbehälter beinhaltend das gefaltete Packstofflaminat mit Auf- und Entladung
WO2017207367A1 (en) * 2016-05-31 2017-12-07 Sig Technology Ag Laminate for dimensionally stable foodstuff containers having an outer polymer layer with a reflectance
DE102017212142A1 (de) * 2017-07-14 2019-01-17 Sig Technology Ag Flächenförmiger Verbund, insbesondere zum Herstellen formstabiler Nahrungsmittelbehälter, beinhaltend eine Polymerschicht P mit einem L-Wert
DE102017212144A1 (de) * 2017-07-14 2019-01-17 Sig Technology Ag Flächenförmiger Verbund, insbesondere zum Herstellen formstabiler Nahrungsmittelbehälter, mit einer ersten und einer weiteren Haftvermittlerschicht, die jeweils einen Acrylatanteil aufweisen
WO2023136220A1 (ja) * 2022-01-11 2023-07-20 凸版印刷株式会社 ガスバリア積層体及び包装袋

Family Cites Families (31)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04503793A (ja) 1989-03-03 1992-07-09 エフビーアイ ブランヅ リミテッド 頂部切妻形容器への腐敗し易い液体の包装方法
IL110356A (en) 1993-07-29 1997-04-15 Int Paper Co Radio-frequency-sealable, non-foil packaging structures
DE19515254C2 (de) * 1995-04-26 1998-06-04 Fresenius Ag PVC-freie Mehrschichtfolie, Verfahren zur Herstellung derselben und deren Verwendung
DE19515599A1 (de) 1995-05-02 1996-11-07 Hoechst Ag Verfahren zur Herstellung von Polypropylenfolien und deren Verwendung
CN1161406C (zh) * 1996-03-21 2004-08-11 森格沃尔德·维帕克尤恩根有限责任公司 多层薄膜、其制备方法及其应用
SE9604687L (sv) 1996-12-19 1998-06-20 Tetra Laval Holdings & Finance Förpackningslaminat, sätt att framställa förpackningslaminatet samt förpackningsbehållare
JP4156073B2 (ja) 1998-04-16 2008-09-24 大日本印刷株式会社 ヒートシール用多層フィルム及びその製造方法並びにそれを用いた紙容器
DE69833480T2 (de) 1998-10-07 2006-08-31 Tetra Laval Holdings & Finance S.A. Verfahren und Vorrichtung zum Herstellen von versiegelten Verpackungen fliessfähiger Nahrungsmittel aus schlauchförmigem Verpackungsmaterial
CN1125756C (zh) * 1999-01-27 2003-10-29 泰特拉-勒维尔金融控股公司 纸容器用层压包装材料及其制成的纸包装容器
WO2001019611A1 (fr) 1999-09-16 2001-03-22 Tetra Laval Holdings & Finance S.A. Materiau lamine pour emballage et son procede de fabrication
SE522090C2 (sv) 2000-10-03 2004-01-13 Tetra Laval Holdings & Finance Förpackningslaminat för en autoklaverbar förpackningsbehållare samt förpackningsbehållare framställd av laminatet
JP4788031B2 (ja) 2000-10-16 2011-10-05 大日本印刷株式会社 紙容器製函用積層材およびそれを使用して製函した紙容器
JP2003221024A (ja) 2002-01-30 2003-08-05 Toppan Printing Co Ltd カップ状容器用積層材料
US20040037983A1 (en) 2002-03-25 2004-02-26 International Paper Company Non-foil barrier laminates
SE523861C2 (sv) 2002-05-07 2004-05-25 Tetra Laval Holdings & Finance Förpackningslaminat, förfarande för tillverkning av detta, samt förpackningsbehållare tillverkad av förpackningslaminatet
JP2004010067A (ja) 2002-06-04 2004-01-15 Nihon Tetra Pak Kk 包装材料、包装容器および包装材料の製造方法
JP4288098B2 (ja) 2003-04-30 2009-07-01 日本マタイ株式会社 紙容器用積層体及びその製造方法
US20050037162A1 (en) 2003-08-11 2005-02-17 Adams John Peter Paperboard laminate for food packaging applications
US20050074621A1 (en) 2003-10-01 2005-04-07 Reighard Tricia Susan Moisture vapor barrier laminate
DE102004055323A1 (de) 2004-11-16 2006-05-18 Cfs Kempten Gmbh Transparente tiefziehfähige Folien mit Antifog-Eigenschaften
SE528259C2 (sv) * 2004-12-22 2006-10-03 Tetra Laval Holdings & Finance Förpackningslaminat, sätt i samband med tillverkning därav, film för dess tilverkning samt en förpackningsbehållare
JP4770186B2 (ja) 2005-01-28 2011-09-14 大日本印刷株式会社 紙容器
RU2401355C2 (ru) 2005-02-10 2010-10-10 Стора Энсо Аб Высококачественный картон и изделия, изготовленные из него
WO2007095667A1 (en) * 2006-02-20 2007-08-30 Huhtamaki New Zealand Limited Improved product packaging
FI123071B (fi) 2006-07-28 2012-10-31 Stora Enso Oyj Eteenimetyyliakrylaattikopolymeerin käyttö D-limoneenin imeytymisen pienentämiseen sitrusmehusta
JP2009073007A (ja) 2007-09-20 2009-04-09 Toppan Printing Co Ltd 紙容器用積層材料及び液体用紙容器
JP5344124B2 (ja) 2008-09-03 2013-11-20 マツダ株式会社 自動車車体の製造方法
RU2535712C2 (ru) 2009-09-11 2014-12-20 Тетра Лаваль Холдингз Энд Файнэнс С.А. Термомеханически стабильная термосвариваемая пленка с барьерным покрытием, упаковочный ламинат, содержащий эту пленку, упаковочный контейнер, образованный из упаковочного ламината, и способ получения пленки
DE102009050419A1 (de) * 2009-10-22 2011-04-28 Sig Technology Ag Perforierter Behälter aus einem flächenförmigen Verbund mit mindestens einer außenseitigen Polyamidschicht sowie ein Verfahren zu dessen Herstellung
CN201587629U (zh) 2009-12-18 2010-09-22 上海界龙实业集团股份有限公司 一种液体无菌复合包装多彩材料
DE202010007972U1 (de) * 2010-07-02 2010-12-09 Kobusch-Sengewald Gmbh Klare transparente Antifog-Mehrschicht-Folie

Also Published As

Publication number Publication date
TR201905854T4 (tr) 2019-05-21
RU2623265C2 (ru) 2017-06-23
MX2014000982A (es) 2014-02-27
IN2014DN00225A (de) 2015-07-10
WO2013013801A1 (en) 2013-01-31
CN103702830B (zh) 2016-08-17
BR112014001723B1 (pt) 2020-06-02
BR112014001723A2 (pt) 2017-02-21
ES2717897T3 (es) 2019-06-26
CN103702830A (zh) 2014-04-02
US9902524B2 (en) 2018-02-27
PL2736716T3 (pl) 2019-07-31
US20140312103A1 (en) 2014-10-23
EP2736716B1 (de) 2019-02-06
DE102011108402A1 (de) 2013-01-31
RU2014101670A (ru) 2015-09-10

Similar Documents

Publication Publication Date Title
US9902524B2 (en) Planar composite with layers of plastic of different Vicat softening temperatures
US9902124B2 (en) Robust planar composite with an intermediate layer of increased vicat softening temperature
EP3166782B1 (de) Flächenförmiger verbund, insbesondere für behälter, mit einer durch verschiedene c=o-gruppenabsorptionsmaxima gekennzeichneten haftvermittlerschicht
EP3463863A1 (de) Behältervorläufer mit formgebungskoeffizient, insbesondere für einen eindimensional stabilen lebensmittel- oder getränkeproduktbehälter
WO2017202912A1 (en) Container precursor with shaping coefficient, especially for a single dimensionally stable food or drink product container
US10399736B2 (en) Planar composite having layers of plastic of different damping properties
US20130196102A1 (en) Container formed from a roll and having improved opening properties as a result of stretching heat treatment of polymer layers
EP3212514B1 (de) Vorrichtung, insbesondere zum verschliessen eines kopfbereichs eines nahrungsmittelbehälters, hergestellt aus einem laminat mit geschältem und umgeschlagenen randbereich
US20150352820A1 (en) Planar composite having layers of plastic from plastics with different damping properties, having a layer comprising lldpe
US11117689B2 (en) Method of producing a container precursor, especially for a single dimensionally stable foodstuff container, without folding over the container precursor
JP7012084B2 (ja) 包装前駆体の縁部領域に作用する発熱装置の手段により包装前駆体を製造するための装置及び方法
US11117341B2 (en) Method of producing a packaging enveloping container precursors, especially each for a single dimensionally stable foodstuff container, with folding over of the container precursor
WO2018041678A1 (en) Sheetlike composite for production of dimensionally stable food and drink product containers having a barrier layer of which the shinier surface faces inward

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20140225

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

DAX Request for extension of the european patent (deleted)
17Q First examination report despatched

Effective date: 20150324

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: EXAMINATION IS IN PROGRESS

RIC1 Information provided on ipc code assigned before grant

Ipc: B32B 7/12 20060101ALN20180713BHEP

Ipc: B32B 27/28 20060101ALN20180713BHEP

Ipc: B32B 7/02 20060101ALI20180713BHEP

Ipc: B32B 3/24 20060101ALN20180713BHEP

Ipc: B32B 27/10 20060101AFI20180713BHEP

Ipc: B32B 15/20 20060101ALN20180713BHEP

Ipc: B32B 27/34 20060101ALN20180713BHEP

Ipc: B32B 27/32 20060101ALN20180713BHEP

Ipc: B32B 27/08 20060101ALN20180713BHEP

Ipc: B32B 15/08 20060101ALN20180713BHEP

Ipc: B65D 5/00 20060101ALN20180713BHEP

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: GRANT OF PATENT IS INTENDED

INTG Intention to grant announced

Effective date: 20180830

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE PATENT HAS BEEN GRANTED

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

REG Reference to a national code

Ref country code: GB

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

Ref country code: AT

Ref legal event code: REF

Ref document number: 1094626

Country of ref document: AT

Kind code of ref document: T

Effective date: 20190215

REG Reference to a national code

Ref country code: DE

Ref legal event code: R096

Ref document number: 602012056455

Country of ref document: DE

REG Reference to a national code

Ref country code: IE

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: NL

Ref legal event code: MP

Effective date: 20190206

REG Reference to a national code

Ref country code: LT

Ref legal event code: MG4D

REG Reference to a national code

Ref country code: ES

Ref legal event code: FG2A

Ref document number: 2717897

Country of ref document: ES

Kind code of ref document: T3

Effective date: 20190626

REG Reference to a national code

Ref country code: DE

Ref legal event code: R082

Ref document number: 602012056455

Country of ref document: DE

Representative=s name: HERZOG IP PATENTANWALTS GMBH, DE

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: FI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190206

Ref country code: NO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190506

Ref country code: LT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190206

Ref country code: NL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190206

Ref country code: PT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190606

Ref country code: SE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190206

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LV

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190206

Ref country code: HR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190206

Ref country code: RS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190206

Ref country code: IS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190606

Ref country code: BG

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190506

Ref country code: GR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190507

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190206

Ref country code: AL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190206

Ref country code: SK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190206

Ref country code: RO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190206

Ref country code: CZ

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190206

Ref country code: EE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190206

REG Reference to a national code

Ref country code: DE

Ref legal event code: R026

Ref document number: 602012056455

Country of ref document: DE

PLBI Opposition filed

Free format text: ORIGINAL CODE: 0009260

PLAX Notice of opposition and request to file observation + time limit sent

Free format text: ORIGINAL CODE: EPIDOSNOBS2

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SM

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190206

26 Opposition filed

Opponent name: TETRA LAVAL HOLDINGS & FINANCE SA

Effective date: 20191106

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MC

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190206

Ref country code: SI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190206

PLAF Information modified related to communication of a notice of opposition and request to file observations + time limit

Free format text: ORIGINAL CODE: EPIDOSCOBS2

REG Reference to a national code

Ref country code: BE

Ref legal event code: MM

Effective date: 20190731

PLBB Reply of patent proprietor to notice(s) of opposition received

Free format text: ORIGINAL CODE: EPIDOSNOBS3

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: BE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20190731

Ref country code: LU

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20190723

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20190723

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: CY

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190206

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190206

Ref country code: HU

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT; INVALID AB INITIO

Effective date: 20120723

REG Reference to a national code

Ref country code: AT

Ref legal event code: UEP

Ref document number: 1094626

Country of ref document: AT

Kind code of ref document: T

Effective date: 20190206

PLBP Opposition withdrawn

Free format text: ORIGINAL CODE: 0009264

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190206

PLBD Termination of opposition procedure: decision despatched

Free format text: ORIGINAL CODE: EPIDOSNOPC1

REG Reference to a national code

Ref country code: DE

Ref legal event code: R100

Ref document number: 602012056455

Country of ref document: DE

PLBM Termination of opposition procedure: date of legal effect published

Free format text: ORIGINAL CODE: 0009276

27C Opposition proceedings terminated

Effective date: 20220919

REG Reference to a national code

Ref country code: GB

Ref legal event code: 732E

Free format text: REGISTERED BETWEEN 20230713 AND 20230719

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: PL

Payment date: 20230626

Year of fee payment: 12

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: TR

Payment date: 20230713

Year of fee payment: 12

Ref country code: IT

Payment date: 20230727

Year of fee payment: 12

Ref country code: GB

Payment date: 20230720

Year of fee payment: 12

Ref country code: ES

Payment date: 20230801

Year of fee payment: 12

Ref country code: CH

Payment date: 20230801

Year of fee payment: 12

Ref country code: AT

Payment date: 20230719

Year of fee payment: 12

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 20230721

Year of fee payment: 12

Ref country code: DE

Payment date: 20230724

Year of fee payment: 12

REG Reference to a national code

Ref country code: ES

Ref legal event code: PC2A

Owner name: SIG COMBIBLOC SERVICES AG

Effective date: 20231130